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Atomfair Methyl 3-bromo-2-fluoropropanoate C4H6BrFO2

Description Methyl 3-bromo-2-fluoropropanoate (CAS No. 399-86-0) is a high-purity fluorinated ester compound with the molecular formula C4H6BrFO2. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive bromo and fluoro functional groups. It is supplied as a clear to pale-yellow liquid with a characteristic ester odor, packaged under inert conditions to ensure stability. Ideal for nucleophilic substitution reactions, cross-coupling reactions, and as a building block for complex fluorinated molecules. Each batch undergoes rigorous QC testing (GC, NMR) to guarantee ??95% purity, making it suitable for demanding laboratory and industrial applications. Store in…

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Description

Description

Methyl 3-bromo-2-fluoropropanoate (CAS No. 399-86-0) is a high-purity fluorinated ester compound with the molecular formula C4H6BrFO2. This specialized chemical is widely utilized in organic synthesis, pharmaceutical research, and material science due to its reactive bromo and fluoro functional groups. It is supplied as a clear to pale-yellow liquid with a characteristic ester odor, packaged under inert conditions to ensure stability. Ideal for nucleophilic substitution reactions, cross-coupling reactions, and as a building block for complex fluorinated molecules. Each batch undergoes rigorous QC testing (GC, NMR) to guarantee ??95% purity, making it suitable for demanding laboratory and industrial applications. Store in a cool, dry place away from light and moisture.

  • CAS No: 399-86-0
  • Molecular Formula: C4H6BrFO2
  • Molecular Weight: 184.99
  • Exact Mass: 183.95352
  • Monoisotopic Mass: 183.95352
  • IUPAC Name: methyl 3-bromo-2-fluoropropanoate
  • SMILES: COC(=O)C(CBr)F
  • Synonyms: methyl 3-bromo-2-fluoropropanoate, 399-86-0, Propanoic acid, 3-bromo-2-fluoro-, methyl ester, DTXSID80399747

Application

Methyl 3-bromo-2-fluoropropanoate serves as a versatile intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its reactive bromo and fluoro groups enable efficient participation in Suzuki-Miyaura and other palladium-catalyzed cross-coupling reactions. Researchers also employ it to introduce fluorinated propanoate motifs into polymers and specialty materials for enhanced chemical resistance.

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